| Identification | More | [Name]
4-Isoquinolineboronic acid | [CAS]
192182-56-2 | [Synonyms]
4-ISOQUINOLINEBORONIC ACID
4-ISOQUINOLINYLBORONI ACID
5-ISOQUINOLINEBORONIC ACID
AKOS BRN-0121
AKOS BRN-0458
CHEMBRDG-BB 4002849
ISOQUINOLIN-4-YLBORONIC ACID
ISOQUINOLIN-5-YLBORONIC ACID
ISOQUINOLINE-4-BORONIC ACID
ISOQUINOLINE-5-BORONIC ACID
RARECHEM AK VD 0025
RARECHEM AK VD 0026
ISOQUINOLYL-4-YL-BORONIC ACID
Isoquinoline-4-boronic acid, 2,2-dimethylpropane-1,3-diol cyclic ester
4-Isoquinolinylboronic acid | [Molecular Formula]
C9H8BNO2 | [MDL Number]
MFCD03839356 | [Molecular Weight]
172.98 | [MOL File]
192182-56-2.mol |
| Chemical Properties | Back Directory | [Melting point ]
178°C | [Boiling point ]
419.1±37.0 °C(Predicted) | [density ]
1.28±0.1 g/cm3(Predicted) | [storage temp. ]
2-8°C | [form ]
solid | [pka]
4.61±0.30(Predicted) | [color ]
White to off-white | [Detection Methods]
HPLC | [InChI]
1S/C9H8BNO2/c12-10(13)9-6-11-5-7-3-1-2-4-8(7)9/h1-6,12-13H | [InChIKey]
GDTOUTKTCGPAGY-UHFFFAOYSA-N | [SMILES]
OB(O)c1cncc2ccccc12 | [CAS DataBase Reference]
192182-56-2(CAS DataBase Reference) |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection . | [WGK Germany ]
WGK 3 | [Hazard Note ]
Irritant | [HazardClass ]
IRRITANT | [HS Code ]
29349990 | [Storage Class]
11 - Combustible Solids | [Hazard Classifications]
Eye Irrit. 2
Skin Irrit. 2
STOT SE 3 |
| Hazard Information | Back Directory | [Chemical Properties]
Pink solid | [Uses]
Reactant for:
- Preparation of selective steroid-11β-hydroxylase (CYP11B1) inhibitors for treatment of cortisol dependent diseases
- Preparation of tetrabutylammonium trifluoroborates
- Preparation of heteroaryl substituted tetrahydropyrroloijquinolinone derivatives as aldosterone synthase inhibitors
- Synthesis of aminoarylpyridazines as selective CB2 agonists for treatment of inflammatory pain
- Preparation of acyl substituted indoles via palladium-catalyzed domino coupling/carbonylation/Suzuki coupling of dibromoethenylanilines
- Synthesis of antagonists of bacterial quorum sensing
- Preparation of potassium heteroaryl trifluoroborates from boronic acids and their use as coupling partners with various aryl and heteroaryl halides in Suzuki-Miyaura cross-coupling reactions
| [General Description]
May contain varying amounts of anhydride |
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